Canonical Allele Identifier: CA1779777481

Gene: HGSNAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43199392G= , CM000670.2:g.43199392G=	GRCh38
NC_000008.10:g.43054535G= , CM000670.1:g.43054535G=	GRCh37
NC_000008.9:g.43173692G=	NCBI36
NG_009552.1:g.63944G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379644.9:c.1731G= MANE Select	ENSP00000368965.4:p.Met577=
ENST00000379644.8:c.1731G=	ENSP00000368965.4:p.Met577=
ENST00000519705.1:n.1047G=
ENST00000521576.1:c.882G=	ENSP00000429029.1:p.Met294=
NM_152419.2:c.1731G=	NP_689632.2:p.Met577=
XM_005273409.1:c.1842G=	XP_005273466.1:p.Met614=
XM_005273410.1:c.1818G=	XP_005273467.1:p.Met606=
XM_005273411.1:c.1650G=	XP_005273468.1:p.Met550=
NM_001363227.1:c.1818G=	NP_001350156.1:p.Met606=
NM_001363228.1:c.1539G=	NP_001350157.1:p.Met513=
NM_001363229.1:c.867G=	NP_001350158.1:p.Met289=
NM_152419.3:c.1731G= MANE Select	NP_689632.2:p.Met577=
NM_001363227.2:c.1818G=	NP_001350156.1:p.Met606=
NM_001363228.2:c.1539G=	NP_001350157.1:p.Met513=
NM_001363229.2:c.867G=	NP_001350158.1:p.Met289=